1,437 research outputs found
PIE: an online prediction system for protein–protein interactions from text
Protein–protein interaction (PPI) extraction has been an important research topic in bio-text mining area, since the PPI information is critical for understanding biological processes. However, there are very few open systems available on the Web and most of the systems focus on keyword searching based on predefined PPIs. PIE (Protein Interaction information Extraction system) is a configurable Web service to extract PPIs from literature, including user-provided papers as well as PubMed articles. After providing abstracts or papers, the prediction results are displayed in an easily readable form with essential, yet compact features. The PIE interface supports more features such as PDF file extraction, PubMed search tool and network communication, which are useful for biologists and bio-system developers. The PIE system utilizes natural language processing techniques and machine learning methodologies to predict PPI sentences, which results in high precision performance for Web users. PIE is freely available at http://bi.snu.ac.kr/pie/
Recommended from our members
A generic approach to behaviour-driven biochemical model construction
This thesis was submitted for the degree of Doctor of Philosophy and awarded by Brunel University.Modelling of biochemical systems has received considerable attention over the last decade from bioengineering, biochemistry, computer science, and mathematics. This thesis investigates the applications of computational techniques to computational systems biology, for the construction of biochemical models in terms of topology and kinetic rates. Due to the complexity of biochemical systems, it is natural to construct models representing the biochemical systems incrementally in a piecewise manner. Syntax and semantics of two patterns are defined for the instantiation of components which are extendable, reusable and fundamental building blocks for models composition. We propose and implement a set of genetic operators and composition rules to tackle issues of piecewise composing models from scratch. Quantitative Petri nets are evolved by the genetic operators, and evolutionary process of modelling are guided by the composition rules. Metaheuristic algorithms are widely applied in BioModel Engineering to support intelligent and heuristic analysis of biochemical systems in terms of structure and kinetic rates. We illustrate parameters of biochemical models based on Biochemical Systems Theory, and then the topology and kinetic rates of the models are manipulated by employing evolution strategy and simulated annealing respectively. A new hybrid modelling framework is proposed and implemented for the models construction. Two heuristic algorithms are performed on two embedded layers in the hybrid framework: an outer layer for topology mutation and an inner layer for rates optimization. Moreover, variants of the hybrid piecewise modelling framework are investigated. Regarding flexibility of these variants, various combinations of evolutionary operators, evaluation criteria and design principles can be taken into account. We examine performance of five sets of the variants on specific aspects of modelling. The comparison of variants is not to explicitly show that one variant clearly outperforms the others, but it provides an indication of considering important features for various aspects of the modelling. Because of the very heavy computational demands, the process of modelling is paralleled by employing a grid environment, GridGain. Application of the GridGain and heuristic algorithms to analyze biological processes can support modelling of biochemical systems in a computational manner, which can also benefit mathematical modelling in computer science and bioengineering. We apply our proposed modelling framework to model biochemical systems in a hybrid piecewise manner. Modelling variants of the framework are comparatively studied on specific aims of modelling. Simulation results show that our modelling framework can compose synthetic models exhibiting similar species behaviour, generate models with alternative topologies and obtain general knowledge about key modelling features
Evaluation of linguistic features useful in extraction of interactions from PubMed; Application to annotating known, high-throughput and predicted interactions in I2D
Motivation: Identification and characterization of protein–protein interactions (PPIs) is one of the key aims in biological research. While previous research in text mining has made substantial progress in automatic PPI detection from literature, the need to improve the precision and recall of the process remains. More accurate PPI detection will also improve the ability to extract experimental data related to PPIs and provide multiple evidence for each interaction
A Dependency Parsing Approach to Biomedical Text Mining
Biomedical research is currently facing a new type of challenge: an excess of information, both in terms of raw data from experiments and in the number of scientific publications describing their results. Mirroring the focus on data mining techniques to address the issues of structured data, there has recently been great interest in the development and application of text mining techniques to make more effective use of the knowledge contained in biomedical scientific publications, accessible only in the form of natural human language.
This thesis describes research done in the broader scope of projects aiming to develop methods, tools and techniques for text mining tasks in general and for the biomedical domain in particular. The work described here involves more specifically the goal of extracting information from statements concerning relations of biomedical entities, such as protein-protein interactions. The approach taken is one using full parsing—syntactic analysis of the entire structure of sentences—and machine learning, aiming to develop reliable methods that can further be generalized to apply also to other domains.
The five papers at the core of this thesis describe research on a number of distinct but related topics in text mining. In the first of these studies, we assessed the applicability of two popular general English parsers to biomedical text mining and, finding their performance limited, identified several specific challenges to accurate parsing of domain text. In a follow-up study focusing on parsing issues related to specialized domain terminology, we evaluated three lexical adaptation methods. We found that the accurate resolution of unknown words can considerably improve parsing performance and introduced a domain-adapted parser that reduced the error rate of theoriginal by 10% while also roughly halving parsing time.
To establish the relative merits of parsers that differ in the applied formalisms and the representation given to their syntactic analyses, we have also developed evaluation methodology, considering different approaches to establishing comparable dependency-based evaluation results. We introduced a methodology for creating highly accurate conversions between different parse representations, demonstrating the feasibility of unification of idiverse syntactic schemes under a shared, application-oriented representation. In addition to allowing formalism-neutral evaluation, we argue that such unification can also increase the value of parsers for domain text mining. As a further step in this direction, we analysed the characteristics of publicly available biomedical corpora annotated for protein-protein interactions and created tools for converting them into a shared form, thus contributing also to the unification of text mining resources. The introduced unified corpora allowed us to perform a task-oriented comparative evaluation of biomedical text mining corpora. This evaluation established clear limits on the comparability of results for text mining methods evaluated on different resources, prompting further efforts toward standardization.
To support this and other research, we have also designed and annotated BioInfer, the first domain corpus of its size combining annotation of syntax and biomedical entities with a detailed annotation of their relationships. The corpus represents a major design and development effort of the research group, with manual annotation that identifies over 6000 entities, 2500 relationships and 28,000 syntactic dependencies in 1100 sentences. In addition to combining these key annotations for a single set of sentences, BioInfer was also the first domain resource to introduce a representation of entity relations that is supported by ontologies and able to capture complex, structured relationships.
Part I of this thesis presents a summary of this research in the broader context of a text mining system, and Part II contains reprints of the five included publications.Siirretty Doriast
Biomedical Event Extraction with Machine Learning
Biomedical natural language processing (BioNLP) is a subfield of natural
language processing, an area of computational linguistics concerned with
developing programs that work with natural language: written texts and
speech. Biomedical relation extraction concerns the detection of semantic
relations such as protein-protein interactions (PPI) from scientific texts.
The aim is to enhance information retrieval by detecting relations between
concepts, not just individual concepts as with a keyword search.
In recent years, events have been proposed as a more detailed alternative
for simple pairwise PPI relations. Events provide a systematic, structural
representation for annotating the content of natural language texts. Events
are characterized by annotated trigger words, directed and typed arguments
and the ability to nest other events. For example, the sentence “Protein A
causes protein B to bind protein C” can be annotated with the nested event
structure CAUSE(A, BIND(B, C)). Converted to such formal representations,
the information of natural language texts can be used by computational
applications. Biomedical event annotations were introduced by the
BioInfer and GENIA corpora, and event extraction was popularized by the
BioNLP'09 Shared Task on Event Extraction.
In this thesis we present a method for automated event extraction, implemented
as the Turku Event Extraction System (TEES). A unified graph
format is defined for representing event annotations and the problem of
extracting complex event structures is decomposed into a number of independent
classification tasks. These classification tasks are solved using SVM
and RLS classifiers, utilizing rich feature representations built from full dependency
parsing. Building on earlier work on pairwise relation extraction
and using a generalized graph representation, the resulting TEES system is
capable of detecting binary relations as well as complex event structures.
We show that this event extraction system has good performance, reaching
the first place in the BioNLP'09 Shared Task on Event Extraction.
Subsequently, TEES has achieved several first ranks in the BioNLP'11 and
BioNLP'13 Shared Tasks, as well as shown competitive performance in the
binary relation Drug-Drug Interaction Extraction 2011 and 2013 shared
tasks.
The Turku Event Extraction System is published as a freely available
open-source project, documenting the research in detail as well as making
the method available for practical applications. In particular, in this thesis
we describe the application of the event extraction method to PubMed-scale
text mining, showing how the developed approach not only shows good
performance, but is generalizable and applicable to large-scale real-world
text mining projects.
Finally, we discuss related literature, summarize the contributions of the
work and present some thoughts on future directions for biomedical event
extraction. This thesis includes and builds on six original research publications.
The first of these introduces the analysis of dependency parses that
leads to development of TEES. The entries in the three BioNLP Shared
Tasks, as well as in the DDIExtraction 2011 task are covered in four publications,
and the sixth one demonstrates the application of the system to
PubMed-scale text mining.Siirretty Doriast
Linguistically inspired roadmap for building biologically reliable protein language models
Deep neural-network-based language models (LMs) are increasingly applied to
large-scale protein sequence data to predict protein function. However, being
largely black-box models and thus challenging to interpret, current protein LM
approaches do not contribute to a fundamental understanding of
sequence-function mappings, hindering rule-based biotherapeutic drug
development. We argue that guidance drawn from linguistics, a field specialized
in analytical rule extraction from natural language data, can aid with building
more interpretable protein LMs that are more likely to learn relevant
domain-specific rules. Differences between protein sequence data and linguistic
sequence data require the integration of more domain-specific knowledge in
protein LMs compared to natural language LMs. Here, we provide a
linguistics-based roadmap for protein LM pipeline choices with regard to
training data, tokenization, token embedding, sequence embedding, and model
interpretation. Incorporating linguistic ideas into protein LMs enables the
development of next-generation interpretable machine-learning models with the
potential of uncovering the biological mechanisms underlying sequence-function
relationships.Comment: 27 pages, 4 figure
- …